Incidence of Anesthesia-related Adverse Events and Obstetric Complications After Cesarean Delivery

Completed

• Conditions: Anesthesia; Adverse Effect, in Labor and Delivery
• Interventions: Other: Observation

• Registration Number: NCT03391648
• Lead Sponsor: Far Eastern Memorial Hospital

Brief Summary

Recruit the parturients who underwent cesarean delivery at Far Eastern MemorialHospital during 2012-2016. After reviewing medical record related to the pregnancy, demographic data, prenatal exam, laboratory data, indication for cesarean section, perioperative events, etc. will be recorded. Analysis will be focused on incidence, temporal trend, and risk factors of anesthesia-related adverse events and obstetric complications.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2017-12-30
• Study First Submitted QC: 2017-12-30
• Study Start: 2018-01-01
• Study First Posted: 2018-01-05
• Primary Completion: 2018-12-31
• Study Completion: 2018-12-31
• Status Verified: 2019-02
• Last Update Submitted: 2019-02-12
• Last Update Posted: 2019-02-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 505

Inclusion Criteria

• all parturients underwent cesarean section at Far Eastern Memorial Hospital during 2012-2016

Exclusion Criteria

• missing data can't be collect during medical chart review

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Cesarean	Observation	-

Primary Outcome Measures

Name	Time	Method
Incidence of anesthesia-related adverse events	Within 42 days after delivery

Trial Locations

Locations (1)

Far Eastern Memorial Hospital; 🇨🇳 New Taipei City, Taiwan